Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 > > Ok Bee, I need your advice please. I have tried and tried, but I > cannot drink a raw egg. I have trouble with cooked eggs! So a raw > egg is just beyond me. I actually got the dry heaves from thinking > about trying it this morning. I wrote a few weeks ago about my food > aversions. I am definitely willing to give up my vegetarian lifestyle > to do this, because I WANT to do this. But the egg drink, bone broths > (EEWW I can't even eat chicken noodle soup) and organ meats is > something I'm not capable of. I remember liver from my childhood. > Anyway, can I still do this program if I do the supplements, coconut > oil, avoidance of off limit foods and so on? ==>I had a friend years ago that had an aversion to meats, similar to yours. However, she would eat eggs, and cheese. But cheese is a no-no on the candida program. You can still do the program but I cannot guarantee the results. If you cannot stand eating meats and eggs you could try taking tons of dessicated liver tablets, which would help. The best, Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 " You can still do the program but I cannot guarantee the results. If you cannot stand eating meats and eggs you could try taking tons of dessicated liver tablets, which would help. " Bee, I can make myself eat the meats and eggs, just not raw eggs and organs. Cooked eggs are ok I assume? Just not as beneficial as the raw? Thanks so much, Bee <beeisbuzzing2003@...> wrote: > " You can still do the program but I cannot guarantee the results. If you cannot stand eating meats and eggs you could try taking tons of dessicated liver tablets, which would help. " The best, Bee --------------------------------- You rock. That's why Blockbuster's offering you one month of Blockbuster Total Access, No Cost. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 > > " You can still do the program but I cannot guarantee the results. If you cannot stand eating meats and eggs you could try taking tons of dessicated liver tablets, which would help. " > > Bee, I can make myself eat the meats and eggs, just not raw eggs and organs. Cooked eggs are ok I assume? Just not as beneficial as the raw? ==>Hi . Sorry I misunderstood you. Cooked eggs are just as nutritious as raw if the egg yolks are left runny, as in poached eggs. You do not have to eat organs either. Cheers, Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 cholesterol is a myth created by the pharmaceutical companies. It doesn't take much research to discover the facts. Have as many eggs as you like per day (maybe limit it to 2 dozen though...) Here's some reading. Click on the facts to read a detailed analysis. http://www.ravnskov.nu/cholesterol.htm If you are not convinced just take a look at his credentials... quite incredible really. . > > How many eggs is it ok to eat each day? They say if you have high > cholesterol (I do) to not eat eggs more than a couple times a week. I've > been hard boiling them and eating a couple a day. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 > > How many eggs is it ok to eat each day? They say if you have high > cholesterol (I do) to not eat eggs more than a couple times a week. I've > been hard boiling them and eating a couple a day. > > > , Before going on Bee's program I ate a lot of eggs per week and had very low cholesterol. As I started to add Coconut oil ( still before the program) my cholesterol went up but still at 180. Now I gave blood last month and it was 218. After blood tests for my annual physical my HDL ( good cholestrol ) was 107 (over 40 is good) and my LDL (bad cholestrol was 112 (under 130 is good). So all the fat and lots of eggs (about 6 a day) is not hurting me. All my other blood test levels were good after being on the program for 8 months. Thank you Bee. Gratefully, Ellen " -) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2008 Report Share Posted April 9, 2008 > > How many eggs is it ok to eat each day? They say if you have high > cholesterol (I do) to not eat eggs more than a couple times a week. I've > been hard boiling them and eating a couple a day. ==>Hi . In addition to what other members write, see the article " Low Cholesterol on 25 Eggs Per Day " ; http://www.healingnaturallybybee.com/articles/eggs1.php Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2008 Report Share Posted April 9, 2008 Hi Ellen & , Cholesterol will go up while the body is detoxifying. Bee > , > Before going on Bee's program I ate a lot of eggs per week and had > very low cholesterol. As I started to add Coconut oil ( still before > the program) my cholesterol went up but still at 180. Now I gave > blood last month and it was 218. After blood tests for my annual > physical my HDL ( good cholestrol ) was 107 (over 40 is good) and my > LDL (bad cholestrol was 112 (under 130 is good). So all the fat and > lots of eggs (about 6 a day) is not hurting me. All my other blood > test levels were good after being on the program for 8 months. > Thank you Bee. > Gratefully, Ellen " -) > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 10, 2008 Report Share Posted April 10, 2008 The magnesium you get on this diet will also keep cholesterol levels in check. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 15, 2009 Report Share Posted April 15, 2009 have you used the cream.have you checked adrenal fatigue,sex hormones especially progesterone.did you check thyroid. > > Hi all > > I have severe ulcerative colitis. I have been taking LDN now (only med) for 47 days. I have been keeping an LDN journal. I've had a very slight decrease in a couple of my symptoms but nothing really helpful yet. I'm still housebound, watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2 weeks. When I first started taking it I slept not bad but now I haven't had a good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having terrible pressure headaches where I can feel every pulse and heartbeat in my head and ears - the pressure is terrible. Also have vomitted a couple of mornings. Should I stop since it doesn't seem to be helping my UC and now I'm not feeling well from the LDN or should I give it more time? If it doesn't start to kick in soon I'm going to have to start back on Prednisone just to function somewhat normally. > > Thankyou > Deanna > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 15, 2009 Report Share Posted April 15, 2009 Hi Deanna, If you’re taking the LDN capsules try the cream instead that’s what I did and I have UC too, but mild they say and I don’t believe it! I’m on 10mg of pred to get over this bad flare, but that’s helping only a little. I put the cream on my inner wrist and night and rub it in completely. Maybe you can do the cream and back down the dose a little. I’ve started LDN the last week in January and by the mid of February I was on the 4.5mg dose, but switched to the cream. It’s only been a month and a week for the 4.5 dose cream now, I’m still sticking with it. I don’t have trouble sleeping it’s having to go to the bathroom in the middle of the night that gets me. I was doing the antifungal diet and by my 7th days I was in severe diarreah mode that I had to add back some bread and sugar, it was terrible, I got a fissure from it and now my anus burns every single day to a point where no meds help and I’m in tears. I just telling you b/c I know how you feel. My pulse is felt in my rectum that’s how bad the spasms are. I just completed a stool test by Doctors Data and hopefully in a week they can shed some light on my situation. Good luck and I’m praying for you. From: low dose naltrexone [mailto:low dose naltrexone ] On Behalf Of Deanna Sent: Wednesday, April 15, 2009 10:27 AM low dose naltrexone Subject: [low dose naltrexone] Having trouble Hi all I have severe ulcerative colitis. I have been taking LDN now (only med) for 47 days. I have been keeping an LDN journal. I've had a very slight decrease in a couple of my symptoms but nothing really helpful yet. I'm still housebound, watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2 weeks. When I first started taking it I slept not bad but now I haven't had a good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having terrible pressure headaches where I can feel every pulse and heartbeat in my head and ears - the pressure is terrible. Also have vomitted a couple of mornings. Should I stop since it doesn't seem to be helping my UC and now I'm not feeling well from the LDN or should I give it more time? If it doesn't start to kick in soon I'm going to have to start back on Prednisone just to function somewhat normally. Thankyou Deanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 15, 2009 Report Share Posted April 15, 2009 > > Hi all > > I have severe ulcerative colitis. I have been taking LDN now (only med) for 47 days. I have been keeping an LDN journal. I've had a very slight decrease in a couple of my symptoms but nothing really helpful yet. I'm still housebound, watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2 weeks. When I first started taking it I slept not bad but now I haven't had a good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having terrible pressure headaches where I can feel every pulse and heartbeat in my head and ears - the pressure is terrible. Also have vomitted a couple of mornings. Should I stop since it doesn't seem to be helping my UC and now I'm not feeling well from the LDN or should I give it more time? If it doesn't start to kick in soon I'm going to have to start back on Prednisone just to function somewhat normally. > > Thankyou > Deanna >============ Email Dr. Jaquelyn Mccandless for advice before stopping LDN. Do not rule out the possibility of lyme disease. Lyme can cause chronic UC symptoms. You may need to see a lyme literate doctor. First make sure candida yeast and molds or other bacterias are not the culprits. Dr. McCandless can tell you of things you can do to see if your situation improves and can give you her list of tests your doctor can run to check for causing factors. Dr McCandless jmccandless@... or jmccandlessATprodigy.net put the @ sign in place ot the AT Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 15, 2009 Report Share Posted April 15, 2009 It " may " be the filler in the capsule causing some of the problem. I had the same side effects (headache, nausea & vomiting) from the avicel filler. After I switched to the acidolpholus filler, the eide effects were gone. > > Hi all > > I have severe ulcerative colitis. I have been taking LDN now (only med) for 47 days. I have been keeping an LDN journal. I've had a very slight decrease in a couple of my symptoms but nothing really helpful yet. I'm still housebound, watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2 weeks. When I first started taking it I slept not bad but now I haven't had a good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having terrible pressure headaches where I can feel every pulse and heartbeat in my head and ears - the pressure is terrible. Also have vomitted a couple of mornings. Should I stop since it doesn't seem to be helping my UC and now I'm not feeling well from the LDN or should I give it more time? If it doesn't start to kick in soon I'm going to have to start back on Prednisone just to function somewhat normally. > > Thankyou > Deanna > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 15, 2009 Report Share Posted April 15, 2009 Probably should try using LDN transdermal cream. Art --- > > Hi all > > I have severe ulcerative colitis. I have been taking LDN now (only med) for 47 days. I have been keeping an LDN journal. I've had a very slight decrease in a couple of my symptoms but nothing really helpful yet. I'm still housebound, watery painful diarrhea and sometimes blood. Follow the SCD strictly for over a year. I started the LDN at 1.5 mg, then 3 mg and have been at 4.5 mg for about 2 weeks. When I first started taking it I slept not bad but now I haven't had a good nights sleep in ages (maybe 1 - 2 hours/night and very restless) I'm having terrible pressure headaches where I can feel every pulse and heartbeat in my head and ears - the pressure is terrible. Also have vomitted a couple of mornings. Should I stop since it doesn't seem to be helping my UC and now I'm not feeling well from the LDN or should I give it more time? If it doesn't start to kick in soon I'm going to have to start back on Prednisone just to function somewhat normally. > > Thankyou > Deanna > Quote Link to comment Share on other sites More sharing options...
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